FDA Inspection
Cody Laboratories, Inc.Cody Laboratories, Inc. – FDA Inspection, Aug 27, 2010
Record Details
This FDA Inspection record concerns Cody Laboratories, Inc., with an inspection on August 27, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Cody Laboratories, Inc.
- Inspection Date
- August 27, 2010
- Product Type
- Drugs
View Company Profile
ID · 254b4f9b-2d59-416c-bc52-e2e51d3b2efe
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 682313
- FDA center
- Human Drugs
- Project area
- Unapproved and Misbranded Drugs
FDA Citations
2- 21 CFR 211.192Extent of discrepancy, failure investigations
- 21 CFR 211.67(b)Written procedures fail to include
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Cody Laboratories, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| December 8, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 30, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 12, 2012 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 18, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 24, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Cody Laboratories, Inc.
- FDA Inspection 1034453 - 2017-12-08
- FDA Inspection 902313 - 2014-10-30
- FDA Inspection 805118 - 2012-10-12
- FDA Inspection 712399 - 2011-02-18
- FDA Inspection 612683 - 2009-07-24
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.